FDA 510(k) Applications Submitted by EIGEN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K063846 | 12/27/2006 | EIGEN DSA 2000 | EIGEN |
| K162474 | 09/06/2016 | Artemis | EIGEN |
| K173744 | 12/07/2017 | ProFuse CAD | Eigen |
Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact